On the determination of equilibrium constants 1 Marcel Maeder University of Newcastle, Australia.

Slides:



Advertisements
Similar presentations
Bio 98 - Lecture 2 Acid-Base Equilibria, pH and Buffers.
Advertisements

Equilibrium Chemistry
Department of Civil & Environmental Engineering
Chem. 31 – 3/16 Lecture. Announcements I More on Additional Problem + Quiz –When stoichiometry is the same, K sp gives solubility (e.g. K sp (AgCl) =
Ch 6: Good Titrations.
Chapter 18: Equilibria in Solutions of Weak Acids and Bases All weak acids behave the same way in aqueous solution: they partially ionize In terms of the.
Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.
An Introduction to Volumetric Analysis
Chem. 31 – 4/8 Lecture. Announcements I Exam 2 – Monday –Covering Ch. 6 (topics since exam 1), 7, 8-1, 17, and parts of 22 (up to and including retention.
Chemical Buffers Edward A. Mottel Department of Chemistry Rose-Hulman Institute of Technology.
Outline Final Comments on Titrations/Equilibria Titration of Base with a strong acid End-point detection Choice of indicators Titration Curve method Start.
Copyright McGraw-Hill Chapter 17 Acid-Base Equilibria and Solubility Equilibria Insert picture from First page of chapter.
Acids, Bases and Buffers The Br Ø nsted-Lowry definitions of an acid and a base are: Acid: species that donates a proton Base: species that can accept.
Titremetric analysis Dr. Mohammad Khanfar. Concept of Titremetric analysis In general, we utilize certain property of a substance to be analyzed in order.
Spectrophotometry: An Analytical Tool. PGCC CHM 103 Sinex IoIo I Cell with Pathlength, b, containing solution light source detector blank where I o =
Ch. 16: Ionic Equilibria Buffer Solution An acid/base equilibrium system that is capable of maintaining a relatively constant pH even if a small amount.
Titrations Titrations A. Titrations – is an experimental procedure in which a standard solution is used to determine the concentration of an unknown.
Chapter 16: Applications of Aqueous Equilibria Renee Y. Becker Valencia Community College 1.
Chapter Four: Stoichiometry “ Stoichiometry is a branch of chemistry that deals with the quantitative relationships that exist between the reactants and.
Chapter 10 Acids and Bases.
Acids and Bases Chapter 15. Acids Have a sour taste. Vinegar owes its taste to acetic acid. Citrus fruits contain citric acid. React with certain metals.
Chem. 31 – 3/9 Lecture. Announcements I Exam 1 –Will be returned in lab (starting later today) –Not completed while preparing this Cl lab report –Due.
Lecture #26 What’s on the Final?
Carbon cycle observing in the coastal ocean Approaches: Remote-sensing In-water sensing In-water autonomous analysis Ship- or station-based autonomous.
Acids and Bases The concept of acidic and basic solutions is perhaps one of the most important topics in chemistry. Acids and bases affect the properties.
PH calculations. What is pH? pH = - log 10 [H + (aq) ] where [H + ] is the concentration of hydrogen ions in mol dm -3 to convert pH into hydrogen ion.
Acid-Base Equilibria Chapter 16. The common ion effect is the shift in equilibrium caused by the addition of a compound having an ion in common with the.
Aqueous Equilibria Chapter 17 HW problems: 3, 5, 14, 15, 16, 23, 24, 27a, 28a, 31, 37, 43, 45, 51, 57.
Aqueous Equilibria. The __________________________ is the shift in equilibrium caused by the addition of a compound having an ion in common with the dissolved.
Acid-Base Chemistry Arrhenius acid: Substance that dissolves in water and provides H + ions Arrhenius base: Substance that dissolves in water and provides.
Spectrophotometry: An Analytical Tool
Neutralization of Acids and Bases. Titrations Standard Solution Sample Solutio n Burett e Primary Standard with a precisely known [ ] Unknown [ ] Sample.
Acids & Bases Chemistry 6.0. Naming Acids Review: A. Binary – H +one anion Prefix “hydro”+ anion name +“ic”acid Ex) HCl hydrochloric acid Ex) H 3 P hydrophosphoric.
Acid/Base Chemistry Part II CHEM 2124 – General Chemistry II Alfred State College Professor Bensley.
AP Chapter 17 Ionic Equilibria of Weak Electrolytes.
1. 2 Model-based analysis for kinetic complexation study of Pizda and Cu(II) Spectrochimica Acta Part A M. Vosough, M. Maeder, M. Jalali-Heravi, S.E.
Acids, Bases, and pH. Acids and Bases Acids produce H + ions Bases produce OH - ions.
Unit 3 Acids and Bases. Hydrogen ions and pH Ion product constant of water (K w ) H 2 O  H + + OH - In pure water : [H + ] = [OH - ] * [ ] are used to.
Acids and Bases. Acids, Bases and Equilibrium When an acid is dissolved in water, the H + ion (proton) produced by the acid combines with water to produce.
Introduction to Acids and Bases Chapter 19. What is and Acid? Arrhenius Acid Defined as any chemical that increases the concentration of hydrogen ions.
Acids and Bases Part 2 The pH Scale The pH scale is used to describe the concentration of an acidic or basic solution.
Acids and Bases Acids taste sour (citric acid, acetic acid) Bases taste bitter (sodium bicarbonate) There are 3 ways to define acids and bases, you will.
Chemical Data Fitting as a Powerful Chemometric Method.
Titrations. The process of adding measured volumes of an acid or base of known concentrations to an acid or base of unknown concentration until neutralization.
Equilibrium. Chemical equilibrium is the state where the concentration of all reactants and products remain constant with time. At equilibrium, the rate.
Volumetric analysis. Titration.
Acid-Base Titrations End point and equivalence point
Chemical Calculations
The Chemistry of Life: Atoms and Molecules
Chem. 31 – 11/20 Lecture.
Warm-Up What 2 elements besides H and N make up the bulk of living matter? An element has a mass of 207 and has 125 neutrons in its nucleus. How many protons.
Chem. 31 – 11/22 Lecture.
Reactions in Aqueous Solution
Acid/Base and Solubility Equilibrium
Science ideas I need to know
Lewis-Acid Base Chemistry and Complexation Equilibria
Warm-Up What 2 elements besides H and N make up the bulk of living matter? An element has a mass of 207 and has 125 neutrons in its nucleus. How many protons.
How Matter is Organized
Acids and bases.
Part 2: Reactions & Inorganic Compounds
Unit 4: Chemical Equations and Stoichiometry
Unit 4: Chemical Equations and Stoichiometry
Warm-Up What 2 elements besides H and N make up the bulk of living matter? An element has a mass of 207 and has 125 neutrons in its nucleus. How many protons.
Hydronium Ions and Hydroxide Ions
Titration of a Weak Base with a Strong Acid The same principles applied above are also applicable where we have: 1. Before addition of any acid, we have.
Net Ionic Equations Balance the equation
Neutralization of Acids and Bases
Aqueous Equilibria Chapter 17
What are acids and bases?. Monoprotic and diprotic acids Many acids are called monoprotic acids. This means that they only donate one mole of protons.
Presentation transcript:

On the determination of equilibrium constants 1 Marcel Maeder University of Newcastle, Australia

Chemometrics The ultimate goal of curve resolution would be to be able to determine the number of components in an overlapping chromatographic peak as well as the spectrum and concentration profile of each compound, without assumption regarding peak shape, location, or identity. Michael F. Delaney: Chemometrics Anal. Chem. 1984, 56, 261R-277R 2

The law of mass action 3 X, Y, Z are called components All X x Y y Z z are called species (components X, Y, Z are also species)

4 If [X x Y y Z z ], [X], [Y] and [Z] are known, the determination of β xyz is very easy. However this is rarely the case. The law of mass action

Case 1: Fe 3+ /SCN - 5 Only Fe(SCN) 2+ absorbs in the visible. If its molar absorptivity ε is known, it is possible to determine [Fe(SCN) 2+ ] from absorbance. Further, [Fe 3+ ] tot and [SCN - ] tot are known, thus: [Fe 3+ ]= [Fe 3+ ] tot - [Fe(SCN) 2+ ] [SCN - ]= [SCN - ] tot - [Fe(SCN) 2+ ]

Case 1: Fe 3+ /SCN - 6 Issue: how can ε be determined? Large excess of SCN -, then all Fe 3+ exists as [Fe(SCN) 2+ ] ??? However, there might/will be formation of [Fe(SCN) 2 + ] which also absorbs with unknown molar absorptivity. We will come back to this system.

Titrations 7 Preparation of a series of solutions with different total concentrations of the components. a) Manual preparation [X] tot,1 [Y] tot,1 [X] tot,1 [X] tot,2 [Y] tot,2 [X] tot,2 [X] tot,3 [Y] tot,3 [X] tot,3 [X] tot,n [Y] tot,n [X] tot,n … One or several properties of each solution are measured e.g. pH UV-Vis spectrum IR spectrum NMR spectrum etc.

Titrations 8 b) automatic preparation One or several properties of each solution are measured e.g. pH UV-Vis spectrum IR spectrum NMR spectrum etc.

Case 2: pH titration 9 The measurement is pH vs addition of reagent pH = -log[H + ], thus the ‘measurement’ is [H + ]

Case 2: pH titration 10 Two protonation equilibria at secondary amines Amide nitrogens are not basic, no protonation H+H+ H+H+ H+H+

Case 2: pH titration 11 Determination of β 110 and β 120 : Systematically change values until the fit is optimal.

Fitting 12 Systematically change parameters until the fit is optimal: a)calculate all species concentrations from total concentrations and initial guesses for equilibrium constants (Newton Raphson) b)Compare computed curve with measured (residuals) c)Change parameters systematically (Newton-Gauss- Marquardt)

Newton-Raphson 13 Example: Cu 2+ ethylene diamine, en protons, H + [Cu 2+ ] tot [en] tot [H] tot [Cu 2+ ], [en], [H]; [enH], [enH 2 ], [Cu(en)], [Cu(en) 2 ], [Cu(en) 3 ], [Cu(en)H], [Cu(en)OH] and [OH - ] need to be calculated

Newton-Raphson species: M, L, and H; HL, H 2 L, ML, ML 2, ML 3, MLH, MLH -1 and OH. 11 equations 1 solution !

Newton-Raphson 15 V_add (mL) LHCu E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E-03 Species Concentrations V_add (mL)L HCuLHLH2CuLCuLOHCuLOH2OH E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E E-03 Component Concentrations

residuals, pH titrations r = pH meas - pH calc 16 pHpH_calc pH calc =-log([H+])

residuals, spectrophotometric titrations R = D meas – D calc D calc = C × A = C × C + D ( = C × C/D) 17 AC R

Newton-Gauss-Marquardt 18

Fitting using the solver (excel) 19 e.g. H 3 PO 4

Fitting using the solver (excel) 20 For 2-component protonation equilibria it is possible to explicitely calculate the volume for a given pH. Calculation of x for a given value of y. Can be done in excel.

Fitting using the solver (excel) 21 The curve is calculated as a function of the parameters

Fitting using the solver (excel) 22 The measured curve is compared with the calculated curve, the parameters are changed until the fit is optimal. Manually or better with solver

Fitting using the solver (excel) 23 The measured curve is compared with the calculated curve, the parameters are changed until the fit is optimal. Manually or better with solver

Fitting using the solver (excel) 24 Fitting only the concentration of the acid

Fitting using the solver (excel) 25 Fitting the concentration of the acid and the protonation constants >>> perfect fit

Example 1 : Fe 3+ /SCN - Fe(SCN) 2+ characteristic dark brown colour, used to detect either Fe 3+ or SCN Inorganica Chimica Acta 445 (2016) 155–159

Example 1 : Fe 3+ /SCN - There are 2 problems: a) potential formation of additional complexes 27

Example 1 : Fe 3+ /SCN - change in λ max is indicative of additional species, rank>1 28

Example 1 : Fe 3+ /SCN - The other problem: b) Complex is not stable, unknown decomposition reactions 29 Absorbance at 458 nm against time for different SCN - concentrations; (a) with a linear, (b) with a logarithmic time scale.

Measurements, stopped- flow [SCN - ] [Fe 3+ ] [HClO 4 ]

Example 1 : Fe 3+ /SCN - solution: Stopped-flow experiment, measure spectrum as a function of time, analyse and calculate spectrum at time=0. 31 Experimental (points) and calculated (lines) absorbances against time for 1.5×10 -4 M Fe 3+ and 0.25 M SCN - ; (a) with a linear, (b) with a logarithmic time scale.

Example 1 : Fe 3+ /SCN - solution: Stopped-flow experiment, measure spectrum as a function of time, analyse and calculate spectrum at time=0. 32

Example 1 : Fe 3+ /SCN - 33 Species concentration against total thiocyanate concentration, total [Fe 3+ ] = 1.5×10 -4 M at ionic strength 0.5 M. Legend: M=Fe 3+ ; ML=FeSCN 2+ ; ML2=Fe(SCN) 2 + ; MOH=FeOH 2+ ; LH=HSCN.

Example 1 : Fe 3+ /SCN - 34 YearRef.TechniqueT/ o CIS/M K 1 /M -1 /nm / L mol -1 cm -1 K 2 /M -1 /nm / L mol -1 cm [2]Spectro [7]Spectro [10]Spectro [5(c)]Spectro [6(a)]Potent [3]Spectro Potent [5(d)]Spectro [5(h)]Spectro [6(b)] Stopped- flow Spcctro [6(c)]Spectro [6(d)]Spectro Current work Spectro, stopped- flow ±14587±1485

Example 1 : Fe 3+ /SCN - 35

Example 2 : MEA + CO 2 36 How can this process be observed and analysed quantitatively?

Example 2 : MEA + CO 2 37 How can this process be observed and analysed quantitatively? a)Potentiometric titration (as there are protonation equilibria) No, reactions too slow b)Spectrophotometric titration, with long equilibration No, no useful spectra (unless IR) c) 1 H-NMR yes

Example 2 : MEA + CO 2 38 Total concentration of MEA, CO 3 2-, H + are known Relative concentrations of MEA/MEAH + and carb - /carbH from NMR integrals

Example 2 : MEA + CO 2 39 [MEA/MEAH + ] [carb - /carbH] o, x, ◊ integrals of peaks _______ fitted curves K 7 = 204 ± 5 log K 8 = 7.49 ± 0.05

Example 2a : MEA + CO 2 40 K 7,NMR = 204 ± 5 Kinetic determination (wait for next presentation ) log K 7,NMR = 2.31 ± 0.01 log K 7,kin = 2.69 ± 0.02 ? 

Example 3: morpholine + CO 2 41

morpholine + carbamate Example 3: morpholine + CO 2

1 H-NMR spectra of Morpholine at 25˚C (Morpholine/Na 2 CO 3 1/2 with different volumes of 5M HCl)

Analysis of the data

Result of the Analysis

carbamate and carbamic acid

Example 4: Cu 2+ + DANA potentiometric titrations

Example 4: Cu 2+ + DANA potentiometric titrations First the protonation of the ligand has to be determined H+H+ H+H+ No protonation of the amide groups

Example 4: Cu 2+ + DANA potentiometric titrations 10ml.005 M DANA in 0.191M HCl Titrated with M NaOH

Example 4: Cu 2+ + DANA potentiometric titrations The model, with fitting results

Example 4: Cu 2+ + DANA potentiometric titrations calculated concentrations vs pH and ml added

Example 4: Cu 2+ + DANA potentiometric titrations 2 nd titration in the presence of Cu 2+

Example 4: Cu 2+ + DANA potentiometric titrations 10ml.005 M DANA, M Cu 2+ in 0.191M HCl Titrated with M NaOH

Example 4: Cu 2+ + DANA potentiometric titrations Fitting both titration curves together

Example 4: Cu 2+ + DANA potentiometric titrations calculated concentrations vs pH and ml added

ReactLab pH gamma L is ethylene diamine, H 2 N-CH 2 -CH 2 -NH 2 Activities not concentrations: {L} not [L]

ReactLab pH gamma

Ammonia as amine for PCC aqueous solutions of amines

Ammonia as amine for PCC Ammonia has many advantages, compared to MEA: high capacity no degradation in presence of O 2 cheap less corrosive low energy requirement Main disadvantage high volatility

Ammonia as amine for PCC Main disadvantage high volatility What can be done about it? Addition of loss supressants organic compounds that form hydrogen bridges metal ions

Ammonia as amine for PCC Addition of metal ions indeed reduces the vapor pressure of ammonia

Ammonia as amine for PCC Calculations with a complete equilibrium model reveals that it is just the reduced free [NH 3 ] that results in the reduced loss, as efficient as using less ammonia

Henry coefficient for CO 2 For a simple gas, nonreactive, H N2 can be calculated if the partial pressure p N2 in the gas phase and the concnetration [N 2 ] in the liquid phase are known. [N 2 ] p N2

Henry coefficient for CO 2 For a reactive gas, like CO 2, the partial pressure p CO2 in the gas phaseis easy to determine but the concentration [CO 2 ] in the liquid phase is very difficult to determine p CO2 [CO 2 ] carbon dioxide [H 2 CO 3 ]carbonic acid [HCO 3 - ] bi-carbonate [CO 3 2- ] carbonate [MEACOOH] carbamic acid [MEACOO - ] carbamate

Henry coefficient for CO 2 The approach chosen by chemical engineers: determine H N2O the ratio r is constant for all solvents H CO2 can be calculated fron H N2O !!!

Henry coefficient for CO 2 The chemistry approach: Calculate [CO 2 ] from all the equilibrium constants and determine H CO2. p CO2 [CO 2 ] carbon dioxide [H 2 CO 3 ]carbonic acid [HCO 3 - ] bi-carbonate [CO 3 2- ] carbonate [MEACOOH] carbamic acid [MEACOO - ] carbamate

Henry coefficient for CO 2 There are some 1000 data sets published many inconsistencies p CO2 [CO 2 ] tot [MEA] tot At many temperatures

Henry coefficient for CO 2 many inconsistencies: p CO2 [CO 2 ] tot 0-3 M [MEA] tot 2.5 M 40 C

Henry coefficient for CO 2 many inconsistencies: p CO2 [CO 2 ] tot 0-3 M [MEA] tot M C

Chemistry - Metrics Michael F. Delaney: Chemometrics Anal. Chem. 1984, 56, 261R-277R 70

kheili mamnoon 71

kheili mamnoon 72

73 CbCb C a, V a pH